Cruz-Fernández J M, Bedarida G V, Adgey J, Allen C, Johnson-Levonas A O, Massaad R
Universidad de Sevilla, Sevilla, Spain.
Int J Clin Pract. 2005 Jun;59(6):619-27. doi: 10.1111/j.1368-5031.2005.00565.x.
This randomised, double-blind, placebo (PBO)-controlled study evaluated the efficacy and safety of ezetimibe (EZE) co-administered with ongoing atorvastatin (ATV) therapy in 450 hypercholesterolemic patients with coronary heart disease (CHD) who had not achieved their low-density lipoprotein cholesterol (LDL-C) goal < or =2.60 mmol/l while on a stable dose of ATV 10 or 20 mg/day for > or =6 weeks. After a 4-week diet/baseline active run-in period, patients with LDL-C >2.60 mmol/l and < or =4.20 mmol/l were stratified by ATV dose and randomised (1 : 1) to EZE 10 mg or PBO for 6 weeks while continuing open-label ATV. Significantly more patients achieved an LDL-C goal < or =2.6 mmol/l with EZE than PBO (81.3 vs. 21.8%; p < or = 0.001). Compared to PBO, co-administration of EZE with ongoing ATV led to significantly (p < or = 0.001) greater reductions in LDL-C, total cholesterol, triglycerides, non-high-density lipoprotein cholesterol (non-HDL-C), and apolipoprotein B; HDL-C was significantly (p < or = 0.05) increased. Co-administration of EZE and ATV was well tolerated, with an overall safety profile similar to ATV alone.
这项随机、双盲、安慰剂(PBO)对照研究评估了依折麦布(EZE)与正在进行的阿托伐他汀(ATV)治疗联合应用于450例冠心病(CHD)高胆固醇血症患者的疗效和安全性。这些患者在稳定服用每天10或20毫克ATV≥6周的情况下,低密度脂蛋白胆固醇(LDL-C)目标未达到≤2.60毫摩尔/升。在为期4周的饮食/基线活性导入期后,LDL-C>2.60毫摩尔/升且≤4.20毫摩尔/升的患者按ATV剂量分层,并随机(1:1)分为接受10毫克EZE或PBO治疗6周,同时继续开放标签的ATV治疗。与PBO相比,接受EZE治疗达到LDL-C目标≤2.6毫摩尔/升的患者显著更多(81.3%对21.8%;p≤0.001)。与PBO相比,EZE与正在进行的ATV联合应用导致LDL-C、总胆固醇、甘油三酯、非高密度脂蛋白胆固醇(non-HDL-C)和载脂蛋白B显著(p≤0.001)更大幅度降低;高密度脂蛋白胆固醇(HDL-C)显著(p≤0.05)升高。EZE和ATV联合应用耐受性良好,总体安全性与单独使用ATV相似。